Anthraquinone Dye
Anthraquinone, also called anthracenedione or dioxoanthracene, is an aromatic organic compound with formula C14H8O2. Isomers include various quinone derivatives. The term anthraquinone, however refers to the isomer, 9,10-anthraquinone (IUPAC: 9,10-dioxoanthracene) wherein the keto groups are located on the central ring. It is a building block of many dyes and is used in bleaching pulp for papermaking. It is a yellow, highly crystalline solid, poorly soluble in water but soluble in hot organic solvents. It is almost completely insoluble in ethanol near room temperature but 2.25 g will dissolve in 100 g of boiling ethanol. Anthraquinone dye, any of a group of organic dyes having molecular structures based upon that of anthraquinone. The group is subdivided according to the methods best suited to their application to various fibres. An important class of synthetic vat dyes whose structure is based on anthraquinone. The resonance structure from the aromatic rings and the carbonyl groups provide the chromophore. Anthraquinone dyes were first sold commercially in 1901. They are vat dyes that must first be reduced with caustic soda and sodium hydrosulfite to produce a soluble compound, then once impregnated in the fiber and dried, they are oxidized with sodium perborate to form the original colorant. Anthraquinone dyes are lightfast and wash fast.
Anthraquinone, also called anthracenedione or dioxoanthracene, is an aromatic organic compound with the formula C14H8O2. The isomers include various quinone derivatives. The term anthraquinone, however, refers to the isomer 9,10-anthraquinone (IUPAC: 9,10-dioxoanthracene) in which the keto groups are located on the central ring. It is a building block of many dyes and is used in the bleaching of paper pulp. It is a yellow solid, very crystalline, sparingly soluble in water but soluble in hot organic solvents. It is almost completely insoluble in ethanol near room temperature but 2.25 g will dissolve in 100 g of boiling ethanol. Anthraquinone dye, any one of a group of organic dyes having molecular structures based on that of anthraquinone. The group is subdivided according to the methods best suited to their application on different fibers. An important class of synthetic dyes for tanks whose structure is based on anthraquinone. The resonance structure of aromatic rings and carbonyl groups provides the chromophore. Anthraquinone dyes were first sold commercially in 1901. They are vat dyes which must first be reduced with caustic soda and sodium hydrosulfite to produce a soluble compound, then once impregnated in the fiber and dried, they are oxidized with sodium perborate to form the original dye. Anthraquinone dyes are lightfast and wash quickly.
High Impact List of Articles
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pH Variations and Chemometric Assessment of Borehole Water in Orji, Owerri Imo State, Nigeria
Christian Ebere Enyoh, Andrew Wirnkor Verla and Ngozi Jane Egejuru Research Article: Journal of Environmental Analytical Chemistry
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The Effect of Produced Water from Heglig Oil Field on Chemical Additives for Fracturing Fluids
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The Effect of Produced Water from Heglig Oil Field on Chemical Additives for Fracturing Fluids
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Prevalence of Some Heavy Metals in Mango and Pawpaw Found in Dumpsites of Obio/Akpo and Eleme Local Government Areas in River State, Nigeria
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Phytoremediation: An Environmental Friendly Technique - A Review
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Study on the Interaction of Retinoic Acids to Human Serum Albumin by Fluorescence and Circular Dichroism Spectroscopy
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Parametric Study for Adsorption of Sodium Rhodizonate on Chitosan
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Parametric Study for Adsorption of Sodium Rhodizonate on Chitosan
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Assessment of Groundwater Quality and Evolution of Hydrochemical Facies around Tummalapalle Area, Cuddapah District, Andhra Pradesh, South India
Nagaraju A, Sreedhar Y, Kumar KS, Thejaswi A and Sharifi Z Research Article: Journal of Environmental Analytical Chemistry
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Assessment of Groundwater Quality and Evolution of Hydrochemical Facies around Tummalapalle Area, Cuddapah District, Andhra Pradesh, South India
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Adsorption of Tartrazine on Medical Activated Charcoal Tablets under Controlled Conditions
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Conference Proceedings
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L-Proline catalyzed one-pot synthesis of polysubstituted pyridine system that incorporates benzothiazole moiety via sustainable sonochemical approach
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Structure-property relationship of vinyl-terminated oligo (2,6-dimethyl-1,4-phenylene ether)s (OPEs): Seeking a OPE with better properties
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Structure-property relationship of vinyl-terminated oligo (2,6-dimethyl-1,4-phenylene ether)s (OPEs): Seeking a OPE with better properties
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Antimicrobial activity of collagen/silver doped hydroxyapatite composites against gram-pozitive and gram-negative bacteria
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Antimicrobial activity of collagen/silver doped hydroxyapatite composites against gram-pozitive and gram-negative bacteria
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Second-order optical nonlinearity dominated by molecuar configuration and crystal packing structure for organic optical device design
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Second-order optical nonlinearity dominated by molecuar configuration and crystal packing structure for organic optical device design
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Discovery of novel tubulin inhibitors and their synergy with BRAF inhibitors for malignant melanoma
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Computer simulation of electrostatic micropump
Y Rihan and S Aly Posters-Accepted Abstracts: Medicinal Chemistry
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Computer simulation of electrostatic micropump
Y Rihan and S Aly Posters-Accepted Abstracts: Medicinal Chemistry
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